Canonical Allele Identifier: PA2829383559
Gene: PSMD10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3220423
ClinVar RCV Id: RCV004513333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002805.1:p.Gln194His
CA10486669
NM_002814.4:c.582A>C
CA413841701
NM_002814.4:c.582A>T